FDA Recall United States Terminated Historical recordClass II
KEURIG DR PEPPER
- Product
- Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-c…
- Published
- March 22, 2023
- Distribution
- AL, AR, AZ, CA, CO, FL, GA, IA, ID, IL,…
KEURIG DR PEPPER Recall: Product labeled to be Diet and Zero Sugar in the ingredient statement may contain sugar due to an production error.
United States
TerminatedClass II
- Company
- KEURIG DR PEPPER
- Product
- Diet Snapple Tea Peach Tea 16 oz. packaged in PET bottle. Ex…
- Recall date
- December 9, 2021
- Terminated
- June 16, 2022
- Source
- FDA
Reason for recall
Product labeled to be Diet and Zero Sugar in the ingredient statement may contain sugar due to an production error.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Diet Snapple Tea Peach Tea 16 oz. packaged in PET bottle. Expiration Date: February 5, 2022. UPC single bottles: 0 7618300314 5. UPC 12 Pack 0 7618300813 3. | Not published in this source record | 11,970 cases | ALN 09H21 (Time Stamp 18:22-23:59) and ALN 10H21 (Time Stamp 00:00-00:25) |
Distribution
- Distributed to 11 warehouses who then further distributed product to retailer
- institutions
- businesses
- etc. throughout the US.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0361-2022
- Event ID
- 89191
- Status
- Terminated
- Classification
- Class II
- Company
- KEURIG DR PEPPER
- Product description
- Diet Snapple Tea Peach Tea 16 oz. packaged in PET bottle. Expiration Date: February 5, 2022. UPC single bottles: 0 7618300314 5. UPC 12 Pack 0 7618300813 3.
- Quantity
- 11,970 cases
- Reason
- Product labeled to be Diet and Zero Sugar in the ingredient statement may contain sugar due to an production error.
- Recall initiation date
- December 9, 2021
- Report date
- January 12, 2022
- Classification date
- Not published in this source record
- Termination date
- June 16, 2022
- Distribution pattern
- Distributed to 11 warehouses who then further distributed product to retailer, institutions, businesses, etc. throughout the US.
- UPC, lot, and code information
- ALN 09H21 (Time Stamp 18:22-23:59) and ALN 10H21 (Time Stamp 00:00-00:25)
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Letter
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: KEURIG DR PEPPER
Other recalls from KEURIG DR PEPPER
FDA Recall United States Terminated Historical recordClass II
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- Product
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- Published
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- Distribution
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FDA Recall United States Terminated Historical recordClass II
KEURIG DR PEPPER
- Product
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- Published
- December 8, 2021
- Distribution
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Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
